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Formic Acid → 11beta-Formyloxy-androst-4-ene-3,17-dione

HRID 1076291
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HRID 1076291 반응식
[OH:1][C@H:2]1[CH2:19][C@@:17]2([CH3:18])[C@@H:13]([CH2:14][CH2:15][C:16]2=[O:20])[C@H:12]2[C@H:3]1[C@:4]1([CH3:22])[C:9]([CH2:10][CH2:11]2)=[CH:8][C:7](=[O:21])[CH2:6][CH2:5]1.[CH:23](O)=[O:24]>Cl(O)(=O)(=O)=O>[CH:23]([O:1][C@H:2]1[CH2:19][C@@:17]2([CH3:18])[C@@H:13]([CH2:14][CH2:15][C:16]2=[O:20])[C@H:12]2[C@H:3]1[C@:4]1([CH3:22])[C:9]([CH2:10][CH2:11]2)=[CH:8][C:7](=[O:21])[CH2:6][CH2:5]1)=[O:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 284Formic AcidHCID 9414111beta-Hydroxyandrost-4-ene-3,17-dione

생성물 1

HCID 5407368611beta-Formyloxy-androst-4-ene-3,17-dione

시약·촉매·용매 1

HCID 24247Perchloric Acid용매

실험 절차

The starting 11β-formyloxy-androst-4-ene-3,17-dione was prepared from 11β-hydroxy-androst-4-ene-3,17-dione by dissolving the latter in excess formic acid in the presence of a catalytic amount of perchloric acid and, after 20 hours at room temperature, pouring the reaction mixture on ice, extracting with methylene chloride and evaporating. There was obtained a product melting at 139°-139.5° (crystallized from ethyl acetate), [α]D25 = 188° (dioxane).

후처리

  1. additionpouring the reaction mixture on ice
  2. extractionextracting with methylene chloride
  3. customevaporating

출처 및 근거

ORD 기록
ord-eaf3f77e037045739706134295f6bafd
출처 데이터셋
uspto-grants-1976_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03956316

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